Canonical Allele Identifier: CA3711219

Gene: HLA-B

Linked Data

• dbSNP Id: rs147623692
• ExAC: 6:31322421 G / T
• gnomAD v2: 6-31322421-G-T
• gnomAD v3: 6-31354644-G-T
• gnomAD v4: 6-31354644-G-T
• MyVariant Identifiers: chr6:g.31322421G>T (hg19) ; chr6:g.31354644G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354644G>T , CM000668.2:g.31354644G>T	GRCh38
NC_000006.11:g.31322421G>T , CM000668.1:g.31322421G>T	GRCh37
NC_000006.10:g.31430400G>T	NCBI36
NG_023187.1:g.7569C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3081C>A
ENST00000481849.6:n.3041C>A
ENST00000497377.6:n.2948C>A
ENST00000640094.2:c.917C>A	ENSP00000491275.2:p.Ser306Tyr
ENST00000696558.1:c.1103C>A	ENSP00000512716.1:n.1103C>A
ENST00000696559.1:c.1034C>A	ENSP00000512717.1:p.Ser345Tyr
ENST00000696560.1:c.1034C>A	ENSP00000512718.1:p.Ser345Tyr
ENST00000696561.1:c.1034C>A	ENSP00000512719.1:p.Ser345Tyr
ENST00000696562.1:c.1034C>A	ENSP00000512720.1:p.Ser345Tyr
ENST00000412585.7:c.1034C>A MANE Select	ENSP00000399168.2:p.Ser345Tyr
ENST00000640094.1:c.110C>A	ENSP00000491275.1:p.Ser37Tyr
ENST00000412585.6:c.1034C>A	ENSP00000399168.2:p.Ser345Tyr
ENST00000481849.5:n.163C>A
ENST00000497377.5:n.433C>A
NM_005514.6:c.1034C>A	NP_005505.2:p.Ser345Tyr
XM_011514556.1:c.1067C>A	XP_011512858.1:p.Ser356Tyr
XM_011514557.1:c.917C>A	XP_011512859.1:p.Ser306Tyr
XR_926175.1:n.1473C>A
NM_005514.7:c.1034C>A	NP_005505.2:p.Ser345Tyr
NM_005514.8:c.1034C>A MANE Select	NP_005505.2:p.Ser345Tyr